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升麻提取物通过诱导细胞周期停滞和凋亡来抑制肝细胞的增殖。

Cimicifuga foetida extract inhibits proliferation of hepatocellular cells via induction of cell cycle arrest and apoptosis.

作者信息

Tian Ze, Pan Ruile, Chang Qi, Si Jianyong, Xiao Peigen, Wu Erxi

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100094, China.

出版信息

J Ethnopharmacol. 2007 Nov 1;114(2):227-33. doi: 10.1016/j.jep.2007.08.008. Epub 2007 Aug 12.

Abstract

The purpose of this study is to determine whether the ethyl acetate fraction (EAF) from the aerial part of Cimicifuga foetida Linnaeus possesses the anti-tumor action on hepatoma, and therefore, provide evidence for the traditional use of the plant as a detoxification agent. EAF was extracted and its cytotoxicity was evaluated on a panel of Hepatocytes by MTT assay. The IC(50) values of EAF on HepG2, R-HepG2 and primary cultured normal mouse hepatocytes were 21, 43 and 80 microg/mL, respectively. Morphology observation, Annexin V-FITC/PI staining, cell cycle analysis and western blot were used to further elucidate the cytotoxic mechanism of EAF. EAF induced G(0)/G(1)cell cycle arrest at lower concentration (25 microg/mL), and triggered G(2)/M arrest and apoptosis at higher concentrations (50 and 100 microg/mL, respectively). An increase in the ratio of Bax/Bcl-2, activation of downstream effector Caspase 3, and cleavage of poly-ADP-ribose polymerase (PARP) were implicated in EAF-induced apoptosis. In addition, EAF inhibited the growth of the implanted mouse H(22) tumor in a dose-dependent manner with the growth inhibitory rate of 63.32% at 200 mg/kg. In conclusion, EAF may potentially find use as a new therapy for the treatment of hepatoma.

摘要

本研究旨在确定升麻地上部分的乙酸乙酯提取物(EAF)对肝癌是否具有抗肿瘤作用,从而为该植物作为解毒剂的传统用途提供依据。提取EAF,并通过MTT法在一组肝细胞上评估其细胞毒性。EAF对HepG2、R-HepG2和原代培养的正常小鼠肝细胞的IC(50)值分别为21、43和80微克/毫升。采用形态学观察、Annexin V-FITC/PI染色、细胞周期分析和蛋白质免疫印迹法进一步阐明EAF的细胞毒性机制。EAF在较低浓度(25微克/毫升)时诱导G(0)/G(1)期细胞周期阻滞,在较高浓度(分别为50和100微克/毫升)时引发G(2)/M期阻滞和细胞凋亡。Bax/Bcl-2比值增加、下游效应物半胱天冬酶3激活以及聚ADP核糖聚合酶(PARP)裂解与EAF诱导的细胞凋亡有关。此外,EAF以剂量依赖方式抑制植入的小鼠H(22)肿瘤生长,在200毫克/千克时生长抑制率为63.32%。总之,EAF可能有望成为治疗肝癌的一种新疗法。

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